ODCs

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2 OMIM references -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Paroxysmal kinesigenic dyskinesia

Paroxysmal non-kinesigenic dyskinesia

PRRT2	(UniProt - OMIM)		PNKD	(UniProt - OMIM)
			PRRT2	(UniProt - OMIM)

Citations in the biomedical literature:

Paroxysmal kinesigenic dyskinesia		Paroxysmal non-kinesigenic dyskinesia
	Synonym(s): - Familial PKD - Familial paroxysmal kinesigenic dyskinesia - Paroxysmal kinesigenic choreathetosis		Synonym(s): - Paroxystic non-kinesigenic choreoathetosis

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C537181

No signs/symptoms info available.